Malignancy without immortality? Cellular immortalization as a possible late event in melanoma progression

• Published in: Pigment cell and melanoma research Vol. 24; no. 3; pp. 490 - 503
• Main Authors: Soo, Julia K., MacKenzie Ross, Alastair D., Kallenberg, David M., Milagre, Carla, Heung Chong, W., Chow, Jade, Hill, Lucy, Hoare, Stacey, Collinson, Rebecca S., Hossain, Mehnaz, Keith, W. Nicol, Marais, Richard, Bennett, Dorothy C.
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01-06-2011
• Subjects: Anaphase; Aneuploidy; Biomarkers, Tumor - biosynthesis; cell senescence; Cellular Senescence; crisis; Humans; immortalization; Melanoma - genetics; Melanoma - metabolism; Melanoma - pathology; Neoplasm Proteins - biosynthesis; nevus; Nevus, Pigmented - genetics; Nevus, Pigmented - metabolism; Nevus, Pigmented - pathology; primary melanoma; radial growth-phase; Signaling & Cell Biology; Telomere - genetics; Telomere - metabolism; Telomere - pathology; Tumor Cells, Cultured
• ISSN: 1755-1471; 1755-148X
• DOI: 10.1111/j.1755-148X.2011.00850.x

Summary
Cell senescence is a permanent growth arrest following extended proliferation. Cultured cancer cells including metastatic melanoma cells often appear immortal (proliferate indefinitely), while uncultured benign nevi (moles) show senescence markers. Here, with new explantation methods, we investigated which classes of primary pigmented lesions are typically immortal. Nevi yielded a few proliferating cells, consistent with most nevus cells being senescent. No nevus culture (0/28) appeared immortal. Some thin and thick melanoma cultures proved immortal under these conditions, but surprisingly few (4/37). All arrested cultures displayed three senescence markers in some cells: β‐galactosidase, nuclear p16, and heterochromatic foci/aggregates. However, melanoma cultures also showed features of telomeric crisis (arrest because of ultrashort telomeres). Moreover, crisis markers including anaphase bridges were frequent in uncultured vertical growth‐phase (VGP) melanomas. Conversely, all immortal melanoma cultures expressed telomerase reverse transcriptase and telomerase, showing aneuploidy. The findings suggest that primary melanomas are typically precrisis, with immortalization/telomere maintenance as a late event.